强力霉素硬化治疗淋巴畸形的早期经验

Ju Yeon Lee, J. Namgoong, S. Kim, D. Kim
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摘要

目的:淋巴畸形(LMs)是淋巴系统的先天性畸形,可以通过硬化疗法有效地治疗。本研究旨在评价强力霉素治疗LMs的疗效。方法:回顾性分析2013年3月至2014年2月峨山医疗中心诊断为LMs并接受强力霉素硬化治疗的所有患者的病历。对21例患者进行了35次硬化治疗。手术在全身麻醉下进行。每次治疗后,临床和影像学反应分为完全(病变大小缩小≥80%)、部分(病变大小缩小<80%)或无反应(病变大小未缩小)。结果:男性11例,女性10例。硬化治疗的中位年龄为21个月(范围2-180个月)。最常见的部位是颈面部(52.3%),其次是四肢(28.6%)和躯干(19.0%)。最常见的病变类型为大囊性(71.4%),其次为微囊性(28.5%)。1例(2.8%)皮肤坏死经创面处理后恢复。38%的患者完全缓解,47.6%的患者部分缓解,14.3%的患者无缓解。治疗频率中位数为1(范围1-5)。无应答组包括所有微囊型。结论:强力霉素硬化治疗大囊性LMs安全有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Early Experience of Doxycycline Sclerotherapy for Lymphatic Malformations
Purpose: Lymphatic malformations (LMs) are congenital malformations of the lymphatic system which can be effectively treated by sclerotherapy. This study aims to evaluate the efficacy of doxycycline in the treatment of LMs. Methods: We retrospectively reviewed the medical records of all patients who were diagnosed as LMs and underwent doxycycline sclerotherapy in Asan Medical Center between March 2013 and February 2014. Thirty-five sclerotherapy procedures were performed on 21 patients. The procedures were performed under general anesthesia. After each treatment, the clinical and radiographic response was characterized as complete (≥80% decrease in lesion size), partial (<80% decrease of size), or no response (no decrease of size). Results: There were 11 male patients and 10 female patients. The median age of sclerotherapy was 21 months (range, 2–180 months). The most common location was cervicofacial (52.3%), followed by extremity (28.6%) and truncal (19.0%). The most common lesion type was macrocystic (71.4%), followed by microcystic (28.5%). There was one (2.8%) skin necrosis which was recovered by wound management. Thirty-eight percent of patients had a complete response, 47.6% of patients had a partial response and 14.3% of patients had no response. Median frequency of treatment was one (range, 1–5). No response group consisted of all microcystic type. Conclusion: Sclerotherapy with Doxycycline is safe and effective for macrocystic LMs.
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